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A comprehensive and critical review of state of the art hybrid quantum dots and organic solar cells is presented with the goal of advancing their commercial applications.

Phytophthora root and stem rot is a worldwide soybean (Glycine max) disease caused by the soil-borne pathogen Phytophthora sojae. This disease is devastating to soybean production, so improvement of resistance to P. sojae is a major target in soybean breeding. Mitogen-activated protein kinase (MAPK) cascades are important signaling modules that convert environmental stimuli into cellular responses. Compared with extensive studies in Arabidopsis, the molecular mechanism of MAPK cascades in soybean disease resistance is barely elucidated. In this work, we found that the gene expression of mitogen-activated protein kinase 6 (GmMPK6) was potently induced by P. sojae infection in the disease-resistant soybean cultivar 'Suinong 10'. Overexpression of GmMPK6 in soybean resulted in enhanced resistance to P. sojae and silencing of GmMPK6 led to the opposite phenotype. In our attempt to dissect the role of GmMPK6 in soybean resistance to phytophthora disease, we found that MAPK kinase 4 (GmMKK4) and the ERF transcription factor GmERF113 physically interact with GmMPK6, and we determined that GmMKK4 could phosphorylate and activate GmMPK6, which could subsequently phosphorylate GmERF113 upon P. sojae infection, suggesting that P. sojae can stimulate the GmMKK4-GmMPK6-GmERF113 signaling pathway in soybean. Moreover, phosphorylation of GmERF113 by the GmMKK4-GmMPK6 module promoted GmERF113 stability, nuclear localization and transcriptional activity, which significantly enhanced expression of the defense-related genes GmPR1 and GmPR10-1 and hence improved disease resistance of the transgenic soybean seedlings. In all, our data reveal that the GmMKK4-GmMPK6-GmERF113 cascade triggers resistance to P. sojae in soybean and shed light on functions of MAPK kinases in plant disease resistance.

Aims In agricultural systems, residue amendment is an important practice for nutrient management, but it is not well known how the residue-nitrogen (N) mineralization is associated with changes of microbial community composition in the crop rhizosphere. Therefore, this study aimed to examine the role of microbes in crop residue N mineralization.Methods A rhizobox system was deployed to reveal the gradient change of the residue-N mineralization in the root-growth zone, and 2 mm and 4 mm away from the root of soybean. Plants were grown in a Mollisol without or with amendment of 15N-labelled soybean and maize residues. Furthermore, amplicon sequencing was performed to detect the shift of microbial community composition associated with the residue-N mineralization. Results The residue-N was mineralized faster in the rhizosphere than the bulk soil, and from soybean residue than maize residue. The co-occurrence network of N-mineralization associated community altered with the shift in the hubs. Moreover, greater enrichment of taxa against the unit of residue-N mineralization and more hubs in the network in the soybean than maize residue treatment were correspondent with the enriched ammonification genes, likely contributing to the enhanced mineralization of soybean residue-N in the rhizosphere. An increase in dissolved organic C and a decrease in available N concentration in the rhizosphere, relative to the bulk soil, might shift bacterial community favoring the residue-N mineralization. Conclusions The spatial changes in chemical properties across the rhizosphere lead to the recruitment of core microbiome taxa to enhance the mineralization of N derived from crop residues.

Phytophthora root and stem rot caused by Phytophthora sojae Kaufmann and Gerdemann is a soil-borne disease severely affecting soybean production worldwide. Losses caused by P. sojae can be controlled by both major genes and quantitative trait locus. Here, we tested 112 short-season soybean cultivars from Northeast China for resistance to P. sojae. A total of 58 germplasms were resistant to 7–11 P. sojae strains. Among these, Mengdou 28 and Kejiao 10-262 may harbor either Rps3a or multiple Rps genes conferring resistance to P. sojae. The remaining 110 germplasms produced 91 reaction types and may contain new resistance genes or gene combinations. Partial resistance evaluation using the inoculum layer method revealed that 34 soybean germplasms had high partial resistance, with a mean disease index lower than 30. Combining the results of resistance and partial resistance analyses, we identified 35 excellent germplasm resources as potential elite materials for resistance and tolerance in future breeding programs. In addition, we compared the radicle inoculation method with the inoculum layer method to screen for partial resistance to P. sojae. Our results demonstrate that the radicle inoculation method could potentially replace the inoculum layer method to identify partial resistance against P. sojae, and further verification with larger samples is required in the future.

Phytophthora root rot is a destructive soybean disease worldwide, which is caused by the oomycete pathogen Phytophthora sojae (P. sojae). Wall-associated protein kinase (WAK) genes, a family of the receptor-like protein kinase (RLK) genes, play important roles in the plant signaling pathways that regulate stress responses and pathogen resistance. In our study, we found a putative Glycine max wall-associated protein kinase, GmWAK1, which we identified by soybean GmLHP1 RNA-sequencing. The expression of GmWAK1 was significantly increased by P. sojae and salicylic acid (SA). Overexpression of GmWAK1 in soybean significantly improved resistance to P. sojae, and the levels of phenylalanine ammonia-lyase (PAL), SA, and SA-biosynthesis-related genes were markedly higher than in the wild-type (WT) soybean. The activities of enzymatic superoxide dismutase (SOD) and peroxidase (POD) antioxidants in GmWAK1-overexpressing (OE) plants were significantly higher than those in in WT plants treated with P. sojae; reactive oxygen species (ROS) and hydrogen peroxide (H2O2) accumulation was considerably lower in GmWAK1-OE after P. sojae infection. GmWAK1 interacted with annexin-like protein RJ, GmANNRJ4, which improved resistance to P. sojae and increased intracellular free-calcium accumulation. In GmANNRJ4-OE transgenic soybean, the calmodulin-dependent kinase gene GmMPK6 and several pathogenesis-related (PR) genes were constitutively activated. Collectively, these results indicated that GmWAK1 interacts with GmANNRJ4, and GmWAK1 plays a positive role in soybean resistance to P. sojae via a process that might be dependent on SA and involved in alleviating damage caused by oxidative stress.

Phytophthora root rot is a destructive soybean disease worldwide, which is caused by the oomycete pathogen

Global climate change escalates the rise of atmospheric CO2 concentration and temperature, which impact crop production in agricultural ecosystems. As the second important macronutrient, phosphorus (P) fundamentally mediates the crop adaptability to climate change. An overview on previous work on crop P acquisition and soil P dynamics in responses to elevated CO2 and temperature would be critical for further advancing our knowledge on P cycling under climate change and its management to maintain agroecosystem sustainability. This review focuses on the effects of elevated CO2 and temperature on root morphology, root exudation, and associated biochemical properties in the rhizosphere in relevant to crop P acquisition and soil P availability. Studies indicate that elevated CO2 and temperature could increase P uptake of crops, such as rice and soybean when crops are grown within the range of optimal growth temperature. Elevated CO2 and temperature not only alter root exudates and changes the activity of soil enzymes and microbes the in rhizosphere environment, but also directly influence soil chemical and biochemical processes and thus the bioavailability of P. It is worth to focus on P-solubilizing microbial community composition, and microbial function on soil P mobilization in the rhizosphere of crops grown under climate change.

Crop residue amendment is likely to stimulate symbiotic N2 fixation, and clarifying its effect on N2-fixing bacteria, i.e., diazotrophs in the rhizosphere of legume crops, is important for sustainable N management in legume-cereal cropping systems. Therefore, this study aimed to reveal the diazotrophic community composition in the rhizosphere of soybean in response to maize residue amendment. Being designed with treatments of maize residue, chemical fertilizer, and non-fertilizer applications, this study deployed the 15N-labeling technology combined with high-throughput sequencing of the nifH gene as a molecular marker for diazotrophs to quantify the symbiotically-fixed N2 in soybean plants and link symbiotically fixed N2 to the diazotrophic community diversity in the rhizosphere. Residue amendment increased the abundance of diazotrophs and fundamentally altered the composition of its community in the rhizosphere. It increased the relative abundances of Bradyrhizobium and Azohydromonas compared to the chemical fertilizer treatment. The copy number of nifH in the rhizosphere was associated with dissolved organic carbon and N2 fixation. Residue-induced increase in dissolved organic carbon may provide sufficient carbon sources for diazotroph enrichment and thus enhance nodulation. The maize residue amendment may enrich N2 fixers to facilitate nodulation and subsequent N2 fixation of soybean, highlighting the eco-functional importance of diazotrophs fixing extra N into the rotation system.

Ethylene response factors (ERFs) are involved in biotic and abiotic stress; however, the drought resistance mechanisms of many ERFs in soybeans have not been resolved. Previously, we proved that GmERF113 enhances resistance to the pathogen Phytophthora sojae in soybean. Here, we determined that GmERF113 is induced by 20% PEG-6000. Compared to the wild-type plants, soybean plants overexpressing GmERF113 (GmERF113-OE) displayed increased drought tolerance which was characterized by milder leaf wilting, less water loss from detached leaves, smaller stomatal aperture, lower Malondialdehyde (MDA) content, increased proline accumulation, and higher Superoxide dismutase (SOD) and Peroxidase (POD) activities under drought stress, whereas plants with GmERF113 silenced through RNA interference were the opposite. Chromatin immunoprecipitation and dual effector-reporter assays showed that GmERF113 binds to the GCC-box in the GmPR10-1 promoter, activating GmPR10-1 expression directly. Overexpressing GmPR10-1 improved drought resistance in the composite soybean plants with transgenic hairy roots. RNA-seq analysis revealed that GmERF113 downregulates abscisic acid 8′-hydroxylase 3 (GmABA8’-OH 3) and upregulates various drought-related genes. Overexpressing GmERF113 and GmPR10-1 increased the abscisic acid (ABA) content and reduced the expression of GmABA8’-OH3 in transgenic soybean plants and hairy roots, respectively. These results reveal that the GmERF113-GmPR10-1 pathway improves drought resistance and affects the ABA content in soybean, providing a theoretical basis for the molecular breeding of drought-tolerant soybean.

Phytophthora root and stem rot in soybean [Glycine max (L.) Merr.] is a destructive disease worldwide. Improving soybean resistance to the causal pathogen, Phytophthora sojae, is a major target for breeders; however, it remains largely unclear how the pathogen regulates the various affected signaling pathways in the host, which consist of complex networks including key transcription factors and their targets. We previously demonstrated that GmBTB/POZ enhances soybean resistance to P. sojae and associated defense response. Here, we report that GmBTB/POZ interacts with transcription factor GmAP2 and promotes the ubiquitination of GmAP2. The GmAP2-RNAi transgenic soybean hairy roots exhibited an enhanced resistance to P. sojae, whereas GmAP2-overexpressing hairy roots showed P. sojae hypersensitivity. Subsequently, GmWRKY33 was identified as a target of GmAP2, which represses its expression by directly binding to the GmWRKY33 promoter. GmWRKY33 acts as a positive regulator in the response of soybean to P. sojae. Additionally, the overexpression of GmBTB/POZ released the GmAP2-regulated suppression of GmWRKY33 expression in the GmAP2-OE soybean hairy roots and increased their resistance to P. sojae. Taken together, these results indicate a novel regulatory mechanism, the GmBTB/POZ-GmAP2 modulation of the P. sojae resistance response, which putatively regulates the downstream target gene GmWRKY33 in soybean.

Phytophthora root rot, caused by Phytophthora sojae is a destructive disease of soybean (Glycine max) worldwide. We previously confirmed that the bHLH transcription factor GmPIB1 (P. sojae-inducible bHLH transcription factor) reduces accumulation of reactive oxygen species (ROS) in cells by inhibiting expression of the peroxidase-related gene GmSPOD thus improving the resistance of hairy roots to P. sojae. To identify proteins interacting with GmPIB1 and assess their participation in the defense response to P. sojae, we obtained transgenic soybean hairy roots overexpressing GmPIB1 by Agrobacterium rhizogenes mediated transformation and examined GmPIB1 protein–protein interactions using immunoprecipitation combined with mass spectrometry. We identified 392 proteins likely interacting with GmPIB1 and selected 20 candidate genes, and only 26S proteasome regulatory subunit GmPSMD (Genbank accession no. XP_014631720) interacted with GmPIB1 in luciferase complementation and pull-down experiments and yeast two-hybrid assays. Overexpression of GmPSMD (GmPSMD-OE) in soybean hairy roots remarkably improved resistance to P. sojae and RNA interference of GmPSMD (GmPSMD -RNAi) increased susceptibility. In addition, accumulation of total ROS and hydrogen peroxide (H2O2) in GmPSMD-OE transgenic soybean hairy roots were remarkably lower than those of the control after P. sojae infection. Moreover, in GmPSMD-RNAi transgenic soybean hairy roots, H2O2 and the accumulation of total ROS exceeded those of the control. There was no obvious difference in superoxide anion (O2–) content between control and transgenic hairy roots. Antioxidant enzymes include peroxidase (POD), glutathione peroxidase (GPX), superoxide dismutase (SOD), catalase (CAT) are responsible for ROS scavenging in soybean. The activities of these antioxidant enzymes were remarkably higher in GmPSMD-OE transgenic soybean hairy roots than those in control, but were reduced in GmPSMD-RNAi transgenic soybean hairy roots. Moreover, the activity of 26S proteasome in GmPSMD-OE and GmPIB1-OE transgenic soybean hairy roots was significantly higher than that in control and was significantly lower in PSMD-RNAi soybean hairy roots after P. sojae infection. These data suggest that GmPSMD might reduce the production of ROS by improving the activity of antioxidant enzymes such as POD, SOD, GPX, CAT, and GmPSMD plays a significant role in the response of soybean to P. sojae. Our study reveals a valuable mechanism for regulation of the pathogen response by the 26S proteasome in soybean.

Soybean β-conglycinin α-subunit is an important allergen that adversely affects the nutritional and processing qualities of soya products. Although inheritance of the α-subunit and the molecular basis of α-null mutations have been studied intensively, the molecular mechanism that regulates α-subunit expression remains unclear. Here, we demonstrated that a long intergenic non-coding RNA, acting as a soybean cis-tether terminator1 (designated Linc-GmSTT1) regulate β-conglycinin α-subunit expression. The Linc-GmSTT1 was mapped in physical proximity of α-subunit CG-α-1 gene and demonstrated to be a crucial element of the convergent alpha-transcription termination unit (alpha-TTU). Ingeniously, by reading through, Linc-GmSTT1 and CG-α-1 gene co-transcribed and subsequently achieve its Cgy-2-locus (confirm α-normal) specific regulation function via Linc-GmSTT1-intermolcular interactome. This work provides a unique model whereby LincRNA regulated the effective transcriptional termination of proximal protein-coding genes which might be a crucial procession protecting it from the silencing machinery in plant.

Phytophthora sojae is a destructive pathogen of soybean [Glycine max (L.) Merr.] which causes stem and root rot on soybean plants worldwide. However, the pathogenesis and molecular mechanism of plant defence responses against P. sojae are largely unclear. Herein, we document the underlying mechanisms and function of a novel BTB/POZ protein, GmBTB/POZ, which contains a BTB/POZ domain found in certain animal transcriptional regulators, in host soybean plants in response to P. sojae. It is located in the cell nucleus and is transcriptionally up‐regulated by P. sojae. Overexpression of GmBTB/POZ in soybean resulted in enhanced resistance to P. sojae. The activities and expression levels of enzymatic superoxide dismutase (SOD) and peroxidase (POD) antioxidants were significantly higher in GmBTB/POZ‐overexpressing (GmBTB/POZ‐OE) transgenic soybean plants than in wild‐type (WT) plants treated with sterile water or infected with P. sojae. The transcript levels of defence‐associated genes were also higher in overexpressing plants than in WT on infection. Moreover, salicylic acid (SA) levels and the transcript levels of SA biosynthesis‐related genes were markedly higher in GmBTB/POZ‐OE transgenic soybean than in WT, but there were almost no differences in jasmonic acid (JA) levels or JA biosynthesis‐related gene expression between GmBTB/POZ‐OE and WT soybean lines. Furthermore, exogenous SA application induced the expression of GmBTB/POZ and inhibited the increase in P. sojae biomass in both WT and GmBTB/POZ‐OE transgenic soybean plants. Taken together, these results suggest that GmBTB/POZ plays a positive role in P. sojae resistance and the defence response in soybean via a process that might be dependent on SA.

GmPIB1, previously reported to be up-regulated in Rps near-isogenic lines, enhances resistance to Phytophthora sojae in soybean by repressing expression of GmSPOD1, a key enzyme for producing reactive oxygen species., Phytophthora sojae Kaufmann and Gerdemann causes Phytophthora root rot, a destructive soybean disease worldwide. A basic helix–loop–helix (bHLH) transcription factor is thought to be involved in the response to P. sojae infection in soybean, as revealed by RNA sequencing (RNA-seq). However, the molecular mechanism underlying this response is currently unclear. Here, we explored the function and underlying mechanisms of a bHLH transcription factor in soybean, designated GmPIB1 (P. sojae-inducible bHLH transcription factor), during host responses to P. sojae. GmPIB1 was significantly induced by P. sojae in the resistant soybean cultivar ‘L77-1863’. Analysis of transgenic soybean hairy roots with elevated or reduced expression of GmPIB1 demonstrated that GmPIB1 enhances resistance to P. sojae and reduces reactive oxygen species (ROS) accumulation. Quantitative reverse transcription PCR and chromatin immunoprecipitation–quantitative PCR assays revealed that GmPIB1 binds directly to the promoter of GmSPOD1 and represses its expression; this gene encodes a key enzyme in ROS production. Moreover, transgenic soybean hairy roots with GmSPOD1 silencing through RNA interference exhibited improved resistance to P. sojae and reduced ROS generation. These findings suggest that GmPIB1 enhances resistance to P. sojae by repressing the expression of GmSPOD1.

Crop residue amendment to soil is recommended as an effective management practice to return nutrients, especially in the maize-soybean rotation system where large amounts of maize residues are produced. Quantifying the utilisation of maize-residue N by the subsequent soybean crop is essential for optimising the N fertilisation strategy for sustainable production. However, whether and how maize residue amendment alters N acquisition in soybean plants are largely unknown. It was hypothesised that maize residue would supply N and enhance N2 fixation to meet the N requirements of subsequent soybeans. Three treatments, namely: 1) chemical fertiliser (55.2, 35.2 and 22.4 kg ha−1 of N, P and K, respectively), 2) maize residue (8 t ha−1), and 3) non-fertiliser were applied in a maize-soybean rotation system in a Mollisol soil. It was demonstrated that soybean seed yield in the maize-residue treatment was the same as that in the chemical fertiliser treatment, with 2.9 vs. 3.2 t ha−1 in 2014, 2.7 vs. 2.6 t ha−1 in 2016, and 3.0 vs. 3.1 t ha−1 in 2018. A follow-up pot experiment using 15N-labelled residue indicated that the residue-derived N accounted for 0.5 % of the total N in soybean seeds and the proportion of symbiotically fixed N reached 82 %. The amount of fixed N during the pod-filling period in the residue treatment was 0.66 g plant-1, which was 49 % and 41 % higher than those in the chemical fertiliser and non-fertiliser treatments, respectively. The stimulation of N2 fixation was associated with an increase in fixed N per nodule and the enrichment of diazotrophs in the rhizosphere of soybean. With maize residue amendment, the increased N2-fixing capability of nodules during the reproductive period, rather than residue-derived N, fulfilled the N demand for maintaining seed yield of soybean. In the maize-soybean rotation system, maize residue amendment would facilitate the N2 fixation to partly substitute for N fertiliser for soybean production in Mollisols.

Phytophthora root and stem rot of soybean [Glycine max (L.) Merr.] caused by Phytophthora sojae is a destructive disease worldwide. Phenylalanine ammonia-lyase (PAL) is one of the most extensively studied enzymes related to plant responses to biotic and abiotic stresses. However, the molecular mechanism of PAL in soybean in response to P. sojae is largely unclear. Here, we characterize a novel member of the soybean PAL gene family, GmPAL2.1, which is significantly induced by P. sojae. Overexpression and RNA interference analysis demonstrates that GmPAL2.1 enhances resistance to P. sojae in transgenic soybean plants. In addition, the PAL activity in GmPAL2.1-OX transgenic soybean is significantly higher than that of non-transgenic plants after infection with P. sojae, while that in GmPAL2.1-RNAi soybean plants is lower. Further analyses show that the daidzein, genistein and salicylic acid (SA) levels and the relative content of glyceollins are markedly increased in GmPAL2.1-OX transgenic soybean. Taken together, these results suggest the important role of GmPAL2.1 functioning as a positive regulator in the soybean response to P. sojae infection, possibly by enhancing the content of glyceollins, daidzein, genistein and SA.

Phytophthora sojae is a pathogen that causes stem and root rot in soybean (Glycine max [L.] Merr.). We previously demonstrated that GmBTB/POZ, a BTB/POZ domain-containing nuclear protein, enhances resistance to P. sojae in soybean, via a process that depends on salicylic acid (SA). Here, we demonstrate that GmBTB/POZ associates directly with soybean LIKE HETEROCHROMATIN PROTEIN1 (GmLHP1) in vitro and in vivo and promotes its ubiquitination and degradation. Both overexpression and RNA interference analysis of transgenic lines demonstrate that GmLHP1 negatively regulates the response of soybean to P. sojae by reducing SA levels and repressing GmPR1 expression. The WRKY transcription factor gene, GmWRKY40, a SA-induced gene in the SA signaling pathway, is targeted by GmLHP1, which represses its expression via at least two mechanisms (directly binding to its promoter and impairing SA accumulation). Furthermore, the nuclear localization of GmLHP1 is required for the GmLHP1-mediated negative regulation of immunity, SA levels and the suppression of GmWRKY40 expression. Finally, GmBTB/POZ releases GmLHP1-regulated GmWRKY40 suppression and increases resistance to P. sojae in GmLHP1-OE hairy roots. These findings uncover a regulatory mechanism by which GmBTB/POZ-GmLHP1 modulates resistance to P. sojae in soybean, likely by regulating the expression of downstream target gene GmWRKY40., Zhang et al characterise the mechanism by which GmBTB/POZ enhances resistance to P. sojae in soybean. They show that GmBTB/POZ directly associates with the heterochromatin protein GmLHP1 and mediates its degradation to regulate the salicylic acid signaling pathway, providing insights into the defence against a common soybean disease.

Organic matter application significantly influences soil carbon storage and sequestration in cropland. The investigation of C sequestration through soil organic carbon (SOC) fractions in the soil profile and its relation to nutrient stoichiometry are essential for evaluating the effect of farming practice on soil fertility. This study aimed to examine the effect of cattle manure application on nutrient stoichiometry, which would be associated with soil C stock in SOC fractions, such as microbial biomass C (MBC), dissolved organic C (DOC) and water-soluble organic C (WSOC), coarse particulate organic carbon (cPOC), fine particulate organic carbon (fPOC) and the mineral-associated organic carbon (MOC). A four-year manure application experiment was conducted in a Mollisol, in which fertilization treatments comprised (1) NoF: the non-fertilizer control, (2) F: synthetic fertilizer, i.e. 20.3, 21.2 and 12.2 kg ha−1 of nitrogen (N), phosphorus (P) and potassium (K) in soybean, and 69.0, 28.1 and 6.1 kg ha−1 of N, P and K for corn on an annual basis, respectively, (3) F + M: synthetic fertilizer plus 15 Mg ha-1 of cattle manure and (4) F + 2M: synthetic fertilizer plus 30 Mg ha−1 of cattle manure in a soybean-corn rotation. SOC concentration in top 10 cm of soil was 18 % and 19 % higher under F + M than that under NoF and F, respectively. Whereas, F+2 M significantly increased SOC concentration by 32 %, 32 %, 14 %, and 11 % in 0−10, 10−20, 20−30, and 30−40 cm of soil depth compared to that in respective soil depth under NoF. Compared to NoF and F, manure application (F + M and F+2 M) significantly increased MBC in the top 30 cm of soil depth and DOC concentration in the top 20 cm of soil depth, but significantly decreased WSOC concentration in the top 20 cm of soil depth. F+2 M significantly increased cPOC concentration in the top 30 cm of soil depth compared to NoF and F. F + M significantly increased fPOC concentration in the top 50 cm of soil depth, compared to NoF, and F. F+2 M further increased the fPOC concentration in the top 30 cm of soil depth, compared to F + M. There was no difference among fertilization treatments in MOC concentration in any soil depth. There were significant exponential correlations of C concentration in POC fractions with soil N, P and N/P ratio. These results indicate that the combination of manure and synthetic fertilizer increased C accumulation in the POC fraction especially in the top 30 cm of soil depth. The change of nutrient stoichiometry was responsible to the accumulation of soil organic matter, highlighting that N, rather than P mainly regulated C accumulation in POC. Increasing input of N fertilizer combined with manure application would benefit the formation of soil organic matter in agricultural Mollisols.

Phytophthora root and stem rot, caused by Phytophthora sojae, is an economically important disease of soybean (Glycine max) in Heilongjiang Province, China. The objectives of this research were to determine the race profile of P. sojae in Heilongjiang and evaluate soybean cultivars for reactions to the pathogen races. A total of 96 single-zoospore P. sojae isolates were obtained from soil samples collected from 35 soybean fields in 18 counties in Heilongjiang from 2005 to 2007. Eight races of P. sojae, including races 1, 3, 4, 5, 9, 13, 44, and 54, were identified on a set of eight differentials, each containing a single resistance Rps gene, from 80 of the 96 isolates. Races 1 and 3 were predominant races, comprising 58 and 14 isolates, and representing 60 and 7% of the pathogen population, respectively. Races 4, 5, 44, and 54 were identified for the first time in Heilongjiang, and each was represented by two to three isolates only. Sixty-two soybean cultivars commonly grown in Heilongjiang Province were evaluated for their resistance to the eight P. sojae races identified using the hypocotyl inoculation technique. Based on the percentage of plant mortality rated 5 days after inoculation, 44 cultivars were resistant (

Dendrobium (Dendrobium candidum Wall. ex Lindl.) is a perennial herb in the Orchidaceae family. It has been used as traditional medicinal plant in China, Malaysia, Laos, and Thailand (2). Fungal disease is one of the most important factors affecting the development of Dendrobium production. During summer 2012, chocolate brown spots were observed on leaves of 2-year-old Dendrobium seedlings in a greenhouse in Hangzhou, Zhejiang Province, China, situated at 30.26°N and 120.19°E. Approximately 80% of the plants in each greenhouse were symptomatic. Diseased leaves exhibited irregular, chocolate brown, and necrotic lesions with a chlorotic halo, reaching 0.8 to 3.2 cm in diameter. Affected leaves began to senesce and withered in autumn, and all leaves of diseased plants fell off in the following spring. Symptomatic leaf tissues were cut into small pieces (4 to 5 mm long), surface-sterilized (immersed in 75% ethanol for 30 s, and then 1% sodium hypochlorite for 60 s), rinsed three times in sterilized distilled water, and then cultured on potato dextrose agar (PDA) amended with 30 mg/liter of kanamycin sulfate (dissolved in ddH2O). Petri plates were incubated in darkness at 25 ± 0.5°C, and a grey mycelium with a white border developed after 4 days. Fast-growing white mycelia were isolated from symptomatic leaf samples, and the mycelia became gray-brown with the onset of sporulation after 5 days. Conidia were unicellular, black, elliptical, and 11.4 to 14.3 μm (average 13.1 μm) in diameter. Based on these morphological and pathogenic characteristics, the isolates were tentatively identified as Nigrospora oryzae (1). Genomic DNA was extracted from a representative isolate F12-F, and a ~600-bp fragment was amplified and sequenced using the primers ITS1 and ITS4 (4). BLAST analysis showed that F12-F ITS sequence (Accession No. KF516962) had 99% similarity with the ITS sequence of an N. oryzae isolate (JQ863242.1). Healthy Dendrobium seedlings (4 months old) were used in pathogenicity tests under greenhouse conditions. Leaves were inoculated with mycelial plugs (5 mm in diameter) from a 5-day-old culture of strain F12-F, and sterile PDA plugs served as controls. Seedlings were covered with plastic bags for 5 days and maintained at 25 ± 0.5°C and 80 ± 5% relative humidity. Eight seedlings were used in each experiment, which was repeated three times. After 5 days, typical chocolate brown spots and black lesions were observed on inoculated leaves, whereas no symptoms developed on controls, which fulfilled Koch's postulates. This shows that N. oryzae can cause leaf spot of D. candidum. N. oryzae is a known pathogen for several hosts but has not been previously reported on any species of Dendrobium in China (3). To our knowledge, on the basis of literature, this is the first report of leaf spot of D. candidum caused by N. oryzae in China. References: (1) H. J. Hudson. Trans. Br. Mycol. Soc. 46:355, 1963. (2) Q. Jin et al. PLoS One. 8(4):e62352, 2013. (3) P. Sharma et al. J. Phytopathol. 161:439, 2013. (4) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, 1990.

Excessive nitrogen (N) fertilizer input to agroecosystem fundamentally alters soil microbial properties and subsequent their ecofunctions such as carbon (C) sequestration and nutrient cycling in soil. However, between soils, the rhizobacterial community diversity and structure in response to N addition is not well understood, which is important to make proper N fertilization strategies to alleviate the negative impact of N addition on soil organic C and soil quality and maintain plant health in soils. Thus, a rhizo-box experiment was conducted with soybean grown in two soils, i.e. soil organic C (SOC)-poor and SOC-rich soil, supplied with three N rates in a range from 0 to 100 mg N kg−1. The rhizospheric soil was collected 50 days after sowing and MiSeq sequencing was deployed to analyze the rhizobacterial community structure. The results showed that increasing N addition significantly decreased the number of phylotype of rhizobacteria by 12.3%, and decreased Shannon index from 5.98 to 5.36 irrespective of soils. Compared to the SOC-rich soil, the increases in abundances of Aquincola affiliated to Proteobacteria, and Streptomyces affiliated to Actinobacteria were greater in the SOC-poor soil in response to N addition. An opposite trend was observed for Ramlibacter belong to Proteobacteria. These results suggest that N addition reduced the rhizobacterial diversity and its influence on rhizobacterial community structure was soil-specific.

Nitrogen deficiency limits crop performance under elevated CO2 (eCO2), depending on the ability of plant N uptake. However, the dynamics and redistribution of N2 fixation, and fertilizer and soil N use in legumes under eCO2 have been little studied. Such an investigation is essential to improve the adaptability of legumes to climate change. We took advantage of genotype-specific responses of soybean to increased CO2 to test which N-uptake phenotypes are most strongly related to enhanced yield. Eight soybean cultivars were grown in open-top chambers with either 390 ppm (aCO2) or 550 ppm CO2 (eCO2). The plants were supplied with 100 mg N kg−1 soil as 15N-labeled calcium nitrate, and harvested at the initial seed-filling (R5) and full-mature (R8) stages. Increased yield in response to eCO2 correlated highly (r = 0.95) with an increase in symbiotically fixed N during the R5 to R8 stage. In contrast, eCO2 only led to small increases in the uptake of fertilizer-derived and soil-derived N during R5 to R8, and these increases did not correlate with enhanced yield. Elevated CO2 also decreased the proportion of seed N redistributed from shoot to seeds, and this decrease strongly correlated with increased yield. Moreover, the total N uptake was associated with increases in fixed-N per nodule in response to eCO2, but not with changes in nodule biomass, nodule density, or root length.

The internal transcribed spacer (ITS) region (ITS1, ITS2 and 5.8S rDNA) of the nuclear ribosomal DNA (nrDNA) was amplified via the PCR method in seventeen different isolates of Phytophthora sojae using the common primers of the ITS of fungi. Around 800 bp-1,000 bp fragments were obtained based on the DL2000 marker and the sequences of the PCR products were tested. Taking isolate USA as outgroup, the phylogenetic tree was constructed by means of maximum parsimony analysis, and the genetic evolution among isolates was analyzed. The results showed that there is a great difference between the base constitution of ITS1 and ITS2 among various isolates. The seventeen isolates are classified into three groups, and the isolates from the same region belong to the same group, which shows the variation in geography.

According to the current situation for teaching quality evaluation system in the college of Hunan Urban Construction college, it puts build multi-directional and multisource evaluation system of teaching quality. The system can effectively solve some problems of traditional teaching evaluation, such as: incomplete information collection and incomplete evaluation. This system uses the B/S pattern and the standard three structures: WEB server level, the browser level and database server level. Through this system, it is helpful to reduce respondent burden and to efficiently Collect and use evaluation resources.

Phytophthora root and stem rot of soybean [Glycine max (L.) Merr.], caused by Phytophthora sojae Kaufmann and Gerdemann, is a destructive disease throughout the soybean planting regions in the world. Here, we report insights into the function and underlying mechanisms of a novel ethylene response factor (ERF) in soybean, namely GmERF5, in host responses to P. sojae. GmERF5-overexpressing transgenic soybean exhibited significantly enhanced resistance to P. sojae and positively regulated the expression of the PR10, PR1-1, and PR10-1 genes. Sequence analysis suggested that GmERF5 contains an AP2/ERF domain of 58 aa and a conserved ERF-associated amphiphilic repression (EAR) motif in its C-terminal region. Following stress treatments, GmERF5 was significantly induced by P. sojae, ethylene (ET), abscisic acid (ABA), and salicylic acid (SA). The activity of the GmERF5 promoter (GmERF5P) was upregulated in tobacco leaves with ET, ABA, Phytophthora nicotianae, salt, and drought treatments, suggesting that GmERF5 could be involved not only in the induced defence response but also in the ABA-mediated pathway of salt and drought tolerance. GmERF5 could bind to the GCC-box element and act as a repressor of gene transcription. It was targeted to the nucleus when transiently expressed in Arabidopsis protoplasts. GmERF5 interacted with a basic helix-loop-helix transcription factor (GmbHLH) and eukaryotic translation initiation factor (GmEIF) both in yeast cells and in planta. To the best of our knowledge, GmERF5 is the first soybean EAR motif-containing ERF transcription factor demonstrated to be involved in the response to pathogen infection.

In previous study, a cDNA library enriched for mRNAs encoding ESTs that increased in abundance during infection with Phytophthora sojae was constructed by suppression subtractive hybridization from leaf tissues of a high resistant soybean, and an EST homologous to the class 10 of pathogenesis-related (PR) proteins was identified to be up-regulated by microarray and real-time PCR. Here, the full-length cDNA (termed GmPR10, GenBank accession number FJ960440; ADC31789.1) of the EST was isolated by rapid amplification of cDNA ends, and contains an open reading frame of 474 bp. The GmPR10 protein included a “P-loop’’ motif. The constitutive transcript abundance of GmPR10 in soybean was the highest in leaves, followed by roots and stems. Further analysis showed that GmPR10 mRNA abundance was increased during infection with P. sojae following leaf treatments with gibberellin (GA3), hydrogen peroxide (H2O2), salicylic acid (SA), and abscisic acid (ABA). The dialytically renatured GmPR10 protein significantly inhibited P. sojae hyphal growth and exhibited RNase activity. Transgenic tobacco and soybean plants overexpressing GmPR10 showed increased resistance to P. nicotianae Breda and P. sojae, respectively. These results suggest that the GmPR10 protein plays an important role in host defense against P. sojae infection. To the best of our knowledge, this is the first report on the functional characterization of a PR10 protein from soybean in defense against P. sojae.

Phosphorous (P) deficiency of soils is one of the major yield-limiting factors worldwide. The most economic and efficient strategy for sustainable agriculture is to breed varieties with P-deficiency tolerance. The objective of this study was to map QTLs for P-deficiency tolerance in soybean, which could lay theoretical foundation on molecular marker assisted selection in soybean with improved P-deficiency tolerance. A population consisting of 180 F2:3 lines derived from P-deficiency sensitive soybean variety Kenjian4 and P-deficiency tolerant soybean variety Fengshou24 was developed for mapping QTLs for P-deficiency tolerance. Five agronomic traits of plant height (HT), length of main root (RL), ratio of weight of dry root (DRW) to weight of dry shoot (DSW) (R/S), chlorophyll content in leaves(CHL), and phosphorus uptake of the whole plant (PC) were investigated at seedling stage under P deficiency(-P) and sufficiency(+P) condition in pot trial. All traits segregated continuously in the population under the two conditions. A genetic linkage map consisting of 15 linkage groups was constructed using 86 polymorphic SSR primers. The genetic map spanned 1510.3 cM in length with an average interval of 16.04 cM between adjacent markers. The linkage groups in our study ranged from 211.2 cM in MLG A1 to 10.8 cM in MLG A1, and the number of markers ranged from 10 markers in MLG D1a, MLG D2 and MLG D1b to 2 markers in MLG N. A total of six QTLs associated with P-deficiency tolerance was detected and mapped on MLG D1a, MLG F and MLG O linkage groups for the five traits of HT, LR, CHL, R/S, and PC. Among them, two QTLs had LOD score more than three. All the QTLs explained more than 10% of the total variation, and the additive gene of five QTLs came from Kenjian 4 and that of one QTL from Fengshou 24. An average of 1-2 QTLs were detected for traits related to P-deficiency tolerance using composite interval mapping.